Canonical Allele Identifier: CA10641888
Gene: FGD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 308346
ClinVar RCV Id: RCV000330072
dbSNP Id: rs188648275

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32643900G>T , CM000674.2:g.32643900G>T GRCh38
NC_000012.11:g.32796834G>T , CM000674.1:g.32796834G>T GRCh37
NC_000012.10:g.32688101G>T NCBI36
NG_008626.2:g.249372G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531134.6:c.*3367G>T ENSP00000431323.1:p.=
ENST00000534526.7:c.*3367G>T MANE Select ENSP00000449273.1:p.=
ENST00000427716.6:c.*3367G>T ENSP00000394487.2:p.=
ENST00000494977.1:n.2192-694G>T
NM_001304480.1:c.*3367G>T NP_001291409.1:p.=
NM_001304481.1:c.*3367G>T NP_001291410.1:p.=
NM_001304484.1:c.*3367G>T NP_001291413.1:p.=
NM_139241.3:c.*3367G>T NP_640334.2:p.=
XM_005253304.3:c.*3367G>T XP_005253361.1:p.=
XM_005253307.2:c.*3367G>T XP_005253364.1:p.=
XM_005253308.3:c.*3367G>T XP_005253365.1:p.=
XM_005253309.1:c.*3367G>T XP_005253366.1:p.=
XM_005253310.3:c.*3367G>T XP_005253367.1:p.=
XM_011520554.1:c.*3367G>T XP_011518856.1:p.=
XM_011520555.1:c.*3367G>T XP_011518857.1:p.=
XM_011520556.1:c.*3367G>T XP_011518858.1:p.=
XM_011520557.1:c.*3367G>T XP_011518859.1:p.=
XM_011520558.1:c.*3367G>T XP_011518860.1:p.=
XM_011520559.1:c.*3367G>T XP_011518861.1:p.=
NM_001330373.1:c.*3367G>T NP_001317302.1:p.=
NM_001330374.1:c.*3367G>T NP_001317303.1:p.=
XM_005253304.4:c.*3367G>T XP_005253361.1:p.=
XM_005253308.5:c.*3367G>T XP_005253365.1:p.=
XM_005253310.4:c.*3367G>T XP_005253367.1:p.=
XM_011520558.2:c.*3367G>T XP_011518860.1:p.=
XM_011520559.3:c.*3367G>T XP_011518861.1:p.=
XM_017018803.1:c.2714-694G>T XP_016874292.1:p.=
XM_017018805.1:c.*3367G>T XP_016874294.1:p.=
XM_024448837.1:c.*3367G>T XP_024304605.1:p.=
XM_024448838.1:c.*3367G>T XP_024304606.1:p.=
XM_024448839.1:c.*3367G>T XP_024304607.1:p.=
XM_024448840.1:c.*3367G>T XP_024304608.1:p.=
NM_001370297.1:c.*3367G>T NP_001357226.1:p.=
NM_001370298.1:c.*3367G>T NP_001357227.1:p.=
NM_001304484.2:c.*3367G>T NP_001291413.1:p.=
NM_001330373.2:c.*3367G>T NP_001317302.1:p.=
NM_001330374.2:c.*3367G>T NP_001317303.1:p.=
NM_001370298.3:c.*3367G>T MANE Select NP_001357227.2:p.=
NM_001384126.1:c.2633-694G>T NP_001371055.1:p.=
NM_001384127.1:c.2222-694G>T NP_001371056.1:p.=
NM_001384128.1:c.2222-694G>T NP_001371057.1:p.=
NM_001384130.1:c.*3367G>T NP_001371059.1:p.=
NM_001385118.1:c.*3367G>T NP_001372047.1:p.=